EP3205700A1 - Additising a fuel - Google Patents

Additising a fuel Download PDF

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Publication number
EP3205700A1
EP3205700A1 EP16155208.8A EP16155208A EP3205700A1 EP 3205700 A1 EP3205700 A1 EP 3205700A1 EP 16155208 A EP16155208 A EP 16155208A EP 3205700 A1 EP3205700 A1 EP 3205700A1
Authority
EP
European Patent Office
Prior art keywords
oxygenate
fuel
octane
additive
additised
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP16155208.8A
Other languages
German (de)
English (en)
French (fr)
Inventor
Rana Ali
Sorin Vasile Flip
Brian Edward Macey
John Stuart Rogerson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BP Oil International Ltd
Original Assignee
BP Oil International Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BP Oil International Ltd filed Critical BP Oil International Ltd
Priority to EP16155208.8A priority Critical patent/EP3205700A1/en
Priority to EP17703196.0A priority patent/EP3414304A1/en
Priority to PCT/EP2017/052926 priority patent/WO2017137516A1/en
Priority to MX2018009649A priority patent/MX2018009649A/es
Priority to CN201780011021.5A priority patent/CN109072106A/zh
Priority to EA201891777A priority patent/EA201891777A1/ru
Priority to CA3013661A priority patent/CA3013661A1/en
Priority to AU2017218511A priority patent/AU2017218511A1/en
Priority to BR112018016436-4A priority patent/BR112018016436B1/pt
Priority to SG11201806710VA priority patent/SG11201806710VA/en
Priority to JP2018542192A priority patent/JP2019509372A/ja
Priority to US16/077,450 priority patent/US10927320B2/en
Publication of EP3205700A1 publication Critical patent/EP3205700A1/en
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/10—Use of additives to fuels or fires for particular purposes for improving the octane number
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/023—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
    • C10L1/233—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring containing nitrogen and oxygen in the ring, e.g. oxazoles
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
    • C10L1/233—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring containing nitrogen and oxygen in the ring, e.g. oxazoles
    • C10L1/2335—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring containing nitrogen and oxygen in the ring, e.g. oxazoles morpholino, and derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2200/00—Components of fuel compositions
    • C10L2200/04—Organic compounds
    • C10L2200/0407—Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
    • C10L2200/0415—Light distillates, e.g. LPG, naphtha
    • C10L2200/0423—Gasoline
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2270/00—Specifically adapted fuels
    • C10L2270/02—Specifically adapted fuels for internal combustion engines
    • C10L2270/023—Specifically adapted fuels for internal combustion engines for gasoline engines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/24—Mixing, stirring of fuel components

Definitions

  • This invention relates to a method for additising a fuel.
  • the invention relates to a method for additising a fuel for a spark-ignition internal combustion engine with a non-metallic octane-boosting additive.
  • Spark-ignition internal combustion engines are widely used for power, both domestically and in industry. For instance, spark-ignition internal combustion engines are commonly used to power vehicles, such as passenger cars, in the automotive industry.
  • Methanol and bio-derived ethanol are common oxygenates that are added to fuels to comply with regional regulatory quotas.
  • the oxygenates that are added to fuels are also usually required to meet regional specifications. For instance, in the European Union, ethanol must meet the requirements of EN 15376:2014.
  • a BOB is typically a hydrocarbon-based blendstock which is produced by petroleum refineries and distributed to fuel terminals. The BOB is usually blended in a way which ensures that the distillation profile, octane characteristics and vapour pressure of the oxygenate blended fuel will meet the required regional standards.
  • Standard performance and stability enhancing additives may also be added at the fuel terminal, and the resulting gasoline fuel transported to the retail distribution network, e.g . by road trucks or rail trucks.
  • fuel additives include, e.g., anti-fouling additives such as deposit control/clean-up agents, anti-oxidants, corrosion inhibitors and friction modifiers.
  • anti-fouling additives such as deposit control/clean-up agents, anti-oxidants, corrosion inhibitors and friction modifiers.
  • octane improver additives are also added to the fuel. However, octane improvers are not commonly part of a formulated additive pack as additive packs are primarily used in deposit control and stability.
  • Octane improvers can be used to prevent 'knock', a phenomenon which is caused when the end gas, typically understood to be the unburnt gas between the flame front and combustion chamber walls/piston, ignites spontaneously and bums rapidly and prematurely ahead of the flame front in the combustion chamber, causing the pressure in the cylinder to rise sharply. This creates the characteristic knocking or pinking sound and is known as "knock", "detonation” or "pinking".
  • Gasoline fuels are now required to meet regional and marketing specifications for minimum octane number, and this has led to a demand for octane boosting additives.
  • Organometallic compounds comprising e.g. iron, lead or manganese
  • organometallic octane improvers are well-known octane improvers, with tetraethyl lead (TEL) having been extensively used as a highly effective octane improver.
  • organometallic octane improvers include methylcyclopentadienyl manganese tricarbonyl (MMT) and ferrocene, a compound with the formula Fe(C 5 H 5 ) 2 .
  • MMT methylcyclopentadienyl manganese tricarbonyl
  • ferrocene a compound with the formula Fe(C 5 H 5 ) 2 .
  • octane improvers which are not based on metals include alkylates and aromatic amines, such as N-methyl aniline (NMA).
  • Fuel additives for a fully formulated oxygenated fuel are typically added to the BOB, or the blend of oxygenate and BOB (hereinafter referred to as the oxygenate base fuel), at the fuel terminal.
  • the additives are introduced into the fuel by additive dosing systems just before the fully formulated fuel enters the delivery vehicle (typically a road fuel tanker). This enables different fully formulated fuels to be introduced into each delivery vehicle.
  • the present invention provides a method for preparing a fuel composition which comprises a base fuel, an oxygenate and an octane-boosting additive, said method comprising:
  • a fuel composition which is obtainable by such methods is also provided.
  • the present invention also provides an apparatus comprising:
  • the present invention further provides an additised oxygenate, wherein the additised oxygenate comprises an oxygenate and an octane-boosting additive. Also provided is a method for producing an additised oxygenate, said method comprising blending an octane-boosting additive with an oxygenate.
  • the present invention provides a method for preparing a fuel composition which comprises a base fuel, an oxygenate and an octane-boosting additive.
  • the method comprises blending an additised oxygenate with a base fuel, the additised oxygenate comprising an oxygenate and an octane-boosting additive.
  • the method of the present invention further comprises producing the additised oxygenate by blending the octane-boosting additive with the oxygenate.
  • This may be achieved by adding the octane-boosting additive to an oxygenate storage tank or to an oxygenate stream which leads to a fuel blending point through which the additised oxygenate may be blended with the base fuel.
  • the octane-boosting additive is added to an oxygenate stream which leads to a fuel blending point through which the additised oxygenate may be blended with the base fuel.
  • the additised oxygenate may be passed through a mixing device before it is blended with the base fuel.
  • the fuel composition may be passed through a mixing valve.
  • a single base fuel such as a Blendstock for Oxygenate Blending
  • the method comprises preparing at least two fuels, such as at least four or six fuels, each of the fuels having a different ethanol grade and/or octane number grade.
  • the method comprises blending an octane-boosting additive with an oxygenate to produce a first additised oxygenate, and blending the first additised oxygenate with a base fuel to produce a first fuel composition; and blending the octane-boosting additive with the oxygenate to produce a second additised oxygenate, and blending the second additised oxygenate with the base fuel to produce a second fuel composition; wherein the first and second fuel compositions comprise the same amount of oxygenate but have a different octane number, or the first and second fuel compositions comprise a different amount of oxygenate but have the same octane number.
  • the oxygenate content in the blended fuel is reduced, but with no loss of octane, the volumetric energy density of the fuel improves, thereby providing the user with a fuel economy benefit.
  • the oxygenate that is used in the present invention is preferably suitable for use in a spark-ignition internal combustion engine.
  • suitable oxygenates include alcohols and ethers.
  • Preferred oxygenates are mono-alcohols or mono-ethers with a final boiling point of up to 225 °C, more preferably a mono alcohol containing less than six, more preferably less than five, carbon atoms, e.g . methanol, ethanol, n-propanol, n-butanol, isobutanol, tert-butanol.
  • the oxygenate is methanol, ethanol or butanol, and more preferably ethanol.
  • Suitable ethers include ethers having 5 or more carbon atoms, e.g . methyl tert-butyl ether and ethyl tert-butyl ether.
  • the fuel composition comprises ethanol, e.g . ethanol complying with EN 15376:2014.
  • the oxygenate may be introduced into fuel composition in amount so that the fuel composition meets particular automotive industry standards.
  • the fuel composition may have a maximum oxygen content of 2.7 % by mass.
  • the fuel composition may have maximum amounts of oxygenates as specified in EN 228, e.g. methanol: 3.0 % by volume, ethanol: 5.0 % by volume, iso-propanol: 10.0 % by volume, iso-butyl alcohol: 10.0 % by volume, tert-butanol: 7.0 % by volume, ethers ( e.g . having 5 or more carbon atoms): 10 % by volume and other oxygenates (subject to suitable final boiling point): 10.0 % by volume.
  • the oxygenate is preferably added into the fuel composition so that the fuel composition comprises the oxygenate in an amount of up to 85 %, preferably from 1 % to 30 %, more preferably from 3 % to 20 %, and even more preferably from 5 % to 15 %, by volume.
  • the fuel composition may contain ethanol in an amount of about 5 % by volume ( i.e. an E5 fuel), about 10 % by volume ( i.e. an E10 fuel) or about 15 % by volume ( i.e. an E15 fuel).
  • the octane-boosting additive that is used in the present invention is preferably a non-metallic octane-boosting additive.
  • Preferred additives consist solely of C, H, N and O atoms, with the number of N atoms limited to two, and preferably one per molecule of octane-boosting additive.
  • the non-metallic octane-boosting additive may have a molecular weight of less than 300, preferably less than 250, and more preferably less than 200 g/mole.
  • the octane-boosting additive may have a chemical structure comprising a 6-membered aromatic ring sharing two adjacent aromatic carbon atoms with a 6- or 7-membered saturated heterocyclic ring, the 6- or 7-membered saturated heterocyclic ring comprising a nitrogen atom directly bonded to one of the shared carbon atoms to form a secondary amine and an atom selected from oxygen or nitrogen directly bonded to the other shared carbon atom, the remaining atoms in the 6- or 7-membered heterocyclic ring being carbon (referred to in short as an octane-boosting additive described herein).
  • the octane-boosting additive used in the present invention may be a substituted or unsubstituted 3,4-dihydro-2H-benzo[b][1,4]oxazine (also known as benzomorpholine), or a substituted or unsubstituted 2,3,4,5-tetrahydro-1,5-benzoxazepine.
  • the additive may be 3,4-dihydro-2H-benzo[b][1,4]oxazine or a derivative thereof, or 2,3,4,5-tetrahydro-1,5-benzoxazepine or a derivative thereof.
  • the additive may comprise one or more substituents and is not particularly limited in relation to the number or identity of such substituents.
  • R 2 , R 3 , R 4 , R 5 , R 11 and R 12 are each independently selected from hydrogen and alkyl groups, and preferably from hydrogen, methyl, ethyl, propyl and butyl groups. More preferably, R 2 , R 3 , R 4 , R 5 , R 11 and R 12 are each independently selected from hydrogen, methyl and ethyl, and even more preferably from hydrogen and methyl.
  • R 6 , R 7 , R 8 and R 9 are each independently selected from hydrogen, alkyl and alkoxy groups, and preferably from hydrogen, methyl, ethyl, propyl, butyl, methoxy, ethoxy and propoxy groups. More preferably, R 6 , R 7 , R 8 and R 9 are each independently selected from hydrogen, methyl, ethyl and methoxy, and even more preferably from hydrogen, methyl and methoxy.
  • the octane-boosting additive may be substituted in at least one of the positions represented by R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 , preferably in at least one of the positions represented by R 6 , R 7 , R 8 and R 9 , and more preferably in at least one of the positions represented by R 7 and R 8 . It is believed that the presence of at least one group other than hydrogen may improve the solubility of the octane-boosting additives in a fuel, though the presence of ethanol is also believed to improve the solubility of the octane-boosting additives described herein in the fuel.
  • no more than five, preferably no more than three, and more preferably no more than two, of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 are selected from a group other than hydrogen.
  • one or two of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 ) R 8 , R 9 , R 11 and R 12 are selected from a group other than hydrogen.
  • only one of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 is selected from a group other than hydrogen.
  • R 2 and R 3 are hydrogen, and more preferred that both of R 2 and R 3 are hydrogen.
  • At least one of R 4 , R 5 , R 7 and R 8 is selected from methyl, ethyl, propyl and butyl groups and the remainder of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 are hydrogen. More preferably, at least one of R 7 and R 8 are selected from methyl, ethyl, propyl and butyl groups and the remainder of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 are hydrogen.
  • At least one of R 4 , R 5 , R 7 and R 8 is a methyl group and the remainder of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 are hydrogen. More preferably, at least one of R 7 and R 8 is a methyl group and the remainder of R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 11 and R 12 are hydrogen.
  • X is -O- or -NR 10 -, where R 10 is selected from hydrogen, methyl, ethyl, propyl and butyl groups, and preferably from hydrogen, methyl and ethyl groups. More preferably, R 10 is hydrogen. In preferred embodiments, X is -O-.
  • n may be 0 or 1, though it is preferred that n is 0.
  • Octane-boosting additives that may be used in the present invention include: and
  • Preferred octane-boosting additives include:
  • the fuel composition may comprise a mixture of:
  • references to alkyl groups include different isomers of the alkyl group.
  • references to propyl groups embrace n-propyl and i-propyl groups
  • references to butyl embrace n-butyl, isobutyl, sec-butyl and tert-butyl groups.
  • the octane-boosting additive may be added to the oxygenate with one or more further additives and/or solvent (e.g . those detailed below) in the form of an additive composition.
  • the octane-boosting additive is used in the form of an additive concentrate, optionally comprising solvent or diluent ( e.g . those detailed below).
  • the octane-boosting additive may be introduced into fuel composition in an amount of up to 20 %, preferably from 0.1 % to 10 %, and more preferably from 0.2 % to 5 % weight additive / weight base fuel. Even more preferably, the octane-boosting additive is introduced into the fuel composition in an amount of from 0.25 % to 2 %, and even more preferably still from 0.3 % to 1 % weight additive / weight base fuel. It will be appreciated that, when more than one octane-boosting additive is used, these values refer to the total amount of octane-boosting additive in the fuel.
  • octane-boosting additives described herein may be used in the form of a precursor compound which, under the combustion conditions encountered in an engine, breaks down to form an octane-boosting additive as defined herein.
  • the fuel compositions preferably comprise a major amount (i.e. greater than 50 % by weight) of liquid fuel ("base fuel”) and a minor amount (i.e. less than 50 % by weight) of octane-boosting additive, e.g. octane-boosting additive described herein, i.e.
  • an additive having a chemical structure comprising a 6-membered aromatic ring sharing two adjacent aromatic carbon atoms with a 6- or 7-membered saturated heterocyclic ring, the 6- or 7-membered saturated heterocyclic ring comprising a nitrogen atom directly bonded to one of the shared carbon atoms to form a secondary amine and an atom selected from oxygen or nitrogen directly bonded to the other shared carbon atom, the remaining atoms in the 6-or 7-membered heterocyclic ring being carbon.
  • suitable liquid base fuels include hydrocarbon base fuels, oxygenate base fuels and combinations thereof. It will be appreciated that, although oxygenate components are added to the base fuel, the base fuel itself may also be an oxygenate base fuel. Preferably, the base fuel is a blendstock for oxygenate blending.
  • Hydrocarbon base fuels that may be used in a spark-ignition internal combustion engine may be derived from mineral sources and/or from renewable sources such as biomass ( e.g . biomass-to-liquid sources) and/or from gas-to-liquid sources and/or from coal-to-liquid sources.
  • Oxygenate base fuels that may be used in a spark-ignition internal combustion engine contain oxygenate fuel components, such as alcohols and ethers.
  • Suitable alcohols include straight and/or branched chain alkyl alcohols having from 1 to 6 carbon atoms, e.g . methanol, ethanol, n-propanol, n-butanol, isobutanol, tert-butanol.
  • Preferred alcohols include methanol and ethanol, preferably ethanol.
  • the fuel composition comprises ethanol, e.g . ethanol complying with EN 15376:2014.
  • Suitable ethers include ethers having 5 or more carbon atoms, e.g. methyl tert-butyl ether and ethyl tert-butyl ether.
  • the fuel composition may comprise oxygenates (i.e. from the oxygenate base fuel and the additised oxygenate) in an amount of up to 85 %, preferably from 1 % to 30 %, more preferably from 3 % to 20 %, and even more preferably from 5 % to 15 %, by volume.
  • the fuel may contain ethanol in an amount of about 5 % by volume ( i.e. an E5 fuel), about 10 % by volume ( i.e. an E10 fuel) or about 15 % by volume ( i.e. an E15 fuel).
  • E0 fuel A fuel which is free from ethanol is referred to as an E0 fuel.
  • the fuel compositions disclosed herein are preferably used in a spark-ignition internal combustion engine. It will be appreciated that the fuel compositions may be used in engines other than spark-ignition internal combustion engines, provided that the fuel compositions are suitable for use in a spark-ignition internal combustion engine. Gasoline fuels (including those containing oxygenates) are typically used in spark-ignition internal combustion engines.
  • the fuel composition may meet particular automotive industry standards.
  • the fuel composition may have a maximum oxygen content of 2.7 % by mass.
  • the fuel composition may have maximum amounts of oxygenates as specified in EN 228, e.g. methanol: 3.0 % by volume, ethanol: 5.0 % by volume, iso-propanol: 10.0 % by volume, iso-butyl alcohol: 10.0 % by volume, tert-butanol: 7.0 % by volume, ethers ( e.g. having 5 or more carbon atoms): 10 % by volume and other oxygenates (subject to suitable final boiling point): 10.0 % by volume.
  • ethers e.g. having 5 or more carbon atoms
  • the fuel composition may have a sulfur content of up to 50.0 ppm by weight, e.g. up to 10.0 ppm by weight.
  • suitable fuel compositions include leaded and unleaded fuel compositions.
  • Preferred fuel compositions are unleaded fuel compositions.
  • the fuel composition meets the requirements of EN 228, e.g. as set out in BS EN 228:2012. In other embodiments, the fuel composition meets the requirements of ASTM D 4814, e.g. as set out in ASTM D 4814-15a. It will be appreciated that the fuel compositions may meet both requirements, and/or other fuel standards.
  • the fuel composition for a spark-ignition internal combustion engine may exhibit one or more (such as all) of the following, e.g., as defined according to BS EN 228:2012: a minimum research octane number of 95.0, a minimum motor octane number of 85.0 a maximum lead content of 5.0 mg/l, a density of 720.0 to 775.0 kg/m 3 , an oxidation stability of at least 360 minutes, a maximum existent gum content (solvent washed) of 5 mg/100 ml, a class 1 copper strip corrosion (3 h at 50 °C), clear and bright appearance, a maximum olefin content of 18.0 % by weight, a maximum aromatics content of 35.0 % by weight, and a maximum benzene content of 1.00 % by volume.
  • BS EN 228:2012 a minimum research octane number of 95.0, a minimum motor octane number of 85.0 a maximum lead content of 5.0 mg/l
  • the method comprises adding at least one further fuel additive to the base fuel, preferably by adding the further fuel additive to the blend of additised oxygenate and base fuel e.g. using conventional additisation processes.
  • additives examples include detergents, friction modifiers/anti-wear additives, corrosion inhibitors, combustion modifiers, anti-oxidants, valve seat recession additives, dehazers/demulsifiers, dyes, markers, odorants, anti-static agents, anti-microbial agents, and lubricity improvers.
  • octane improvers may also be introduced into the fuel composition, e.g . octane improvers which are not octane-boosting additives described herein, i.e . they do not have a chemical structure comprising a 6-membered aromatic ring sharing two adjacent aromatic carbon atoms with a 6- or 7-membered saturated heterocyclic ring, the 6- or 7-membered saturated heterocyclic ring comprising a nitrogen atom directly bonded to one of the shared carbon atoms to form a secondary amine and an atom selected from oxygen or nitrogen directly bonded to the other shared carbon atom, the remaining atoms in the 6-or 7-membered heterocyclic ring being carbon.
  • Suitable detergents include polyisobutylene amines (PIB amines) and polyether amines.
  • suitable friction modifiers and anti-wear additives include those that are ash-producing additives or ashless additives.
  • suitable friction modifiers and anti-wear additives include esters ( e.g. glycerol mono-oleate) and fatty acids ( e.g. oleic acid and stearic acid).
  • Suitable corrosion inhibitors include ammonium salts of organic carboxylic acids, amines and heterocyclic aromatics, e.g. alkylamines, imidazolines and tolyltriazoles.
  • Suitable anti-oxidants include phenolic anti-oxidants (e.g. 2,4-di-tertbutylphenol and 3,5-di-tert-butyl-4-hydroxyphenylpropionic acid) and aminic anti-oxidants (e.g . para-phenylenediamine, dicyclohexylamine and derivatives thereof).
  • phenolic anti-oxidants e.g. 2,4-di-tertbutylphenol and 3,5-di-tert-butyl-4-hydroxyphenylpropionic acid
  • aminic anti-oxidants e.g . para-phenylenediamine, dicyclohexylamine and derivatives thereof.
  • valve seat recession additives examples include inorganic salts of potassium or phosphorus.
  • suitable further octane improvers include non-metallic octane improvers include N-methyl aniline and nitrogen-based ashless octane improvers.
  • Metal-containing octane improvers including methylcyclopentadienyl manganese tricarbonyl, ferrocene and tetra-ethyl lead, may also be used.
  • the fuel composition is free of all added metallic octane improvers including methyl cyclopentadienyl manganese tricarbonyl and other metallic octane improvers including e.g ferrocene and tetraethyl lead.
  • dehazers/demulsifiers examples include phenolic resins, esters, polyamines, sulfonates or alcohols which are grafted onto polyethylene or polypropylene glycols.
  • markers and dyes examples include azo or anthraquinone derivatives.
  • Suitable anti-static agents include fuel soluble chromium metals, polymeric sulfur and nitrogen compounds, quaternary ammonium salts or complex organic alcohols.
  • the fuel composition is preferably substantially free from all polymeric sulfur and all metallic additives, including chromium based compounds.
  • the solvent e.g. which has been used to ensure that the additives are in a form in which they can be stored or combined with the liquid fuel, is introduced into the fuel composition.
  • suitable solvents include polyethers and aromatic and/or aliphatic hydrocarbons, e.g. heavy naphtha e.g. Solvesso (Trade mark), xylenes and kerosene.
  • additives Representative typical and more typical independent amounts of additives, (if present) and solvent that may be introduced into the fuel composition are given in the table below.
  • concentrations are expressed by weight (of the base fuel) of active additive compounds, i.e. independent of any solvent or diluent.
  • the total amount of each type of additive is expressed in the table below.
  • the fuel composition comprises or consists of additives and solvents in the typical or more typical amounts recited in the table above.
  • the further fuel additives may also be combined, in one or more steps, with the fuel.
  • the one or more further fuel additives may be combined with the fuel in the form of a refinery additive composition or as a marketing additive composition.
  • the one or more further fuel additives may be combined with one or more other components (e.g. additives and/or solvents) of the fuel composition as a marketing additive, e.g. at a terminal or distribution point.
  • a further fuel additive may also be added on its own at a terminal or distribution point.
  • the one or more further fuel additives may also be combined with one or more other components (e.g . additives and/or solvents) of the fuel composition for sale in a bottle, e.g. for addition to fuel at a later time.
  • the one or more further fuel additives and any other additives of the fuel composition may be incorporated into the fuel composition as one or more additive concentrates and/or additive part packs, optionally comprising solvent or diluent.
  • spark-ignition internal combustion engines include direct injection spark-ignition engines and port fuel injection spark-ignition engines.
  • the spark-ignition internal combustion engine may be used in automotive applications, e.g. in a vehicle such as a passenger car.
  • Suitable direct injection spark-ignition internal combustion engines include boosted direct injection spark-ignition internal combustion engines, e.g. turbocharged boosted direct injection engines and supercharged boosted direct injection engines.
  • Suitable engines include 2.0L boosted direct injection spark-ignition internal combustion engines.
  • Suitable direct injection engines include those that have side mounted direct injectors and/or centrally mounted direct injectors.
  • suitable port fuel injection spark-ignition internal combustion engines include any suitable port fuel injection spark-ignition internal combustion engine including e.g. a BMW 318i engine, a Ford 2.3L Ranger engine and an MB M111 engine.
  • the fuel compositions disclosed herein may be used to increase the octane number of a fuel for a spark-ignition internal combustion engine.
  • the octane-boosting additives increase the RON or the MON of the fuel.
  • the octane-boosting additives increase the RON of the fuel, and more preferably the RON and MON of the fuel.
  • the RON and MON of the fuel may be tested according to ASTM D2699-15a and ASTM D2700-13, respectively.
  • the octane-boosting additives described herein increase the octane number of a fuel for a spark-ignition internal combustion engine, they may also be used to address abnormal combustion that may arise as a result of a lower than desirable octane number.
  • the fuel compositions disclosed herein e.g. those containing octane-boosting additives disclosed herein, may be used for improving the auto-ignition characteristics of a fuel, e.g. by reducing the propensity of a fuel for at least one of auto-ignition, pre-ignition, knock, mega-knock and super-knock, when used in a spark-ignition internal combustion engine.
  • These methods comprise the step of blending an octane-boosting additive described herein with the fuel.
  • the methods described herein may further comprise delivering the blended fuel to a spark-ignition internal combustion engine and/or operating the spark-ignition internal combustion engine.
  • FIG. 1 shows an apparatus (10) in accordance with the present invention.
  • the apparatus comprises a base fuel source (12), an oxygenate source (14) and an octane-boosting additive source (16).
  • the base fuel source (12), oxygenate source (14) and octane-boosting additive source (16) are shown in the figure as storage tanks, though it will be appreciated that these components may e.g. be provided directly from pipelines.
  • An oxygenate is passed from the oxygenate source (14) through an oxygenate feed line (22) to an additive blending point (30).
  • An octane-boosting additive is passed from the octane-boosting additive source (14) through an octane-boosting additive feed line (24) to the additive blending point (30).
  • the oxygenate and the octane-boosting additive are blended to form an additised oxygenate.
  • a base fuel is passed from the base fuel source (12) to a fuel blending point (32).
  • the additised oxygenate is passed through a line (26) to the fuel blending point (32), via a mixing device (34).
  • the additised oxygenate and the base fuel are blended to form a fuel composition.
  • the fuel composition is passed through a line (28) to a fuel composition distribution station (18), via a mixing valve (36).
  • line (24') may be used (as is typical in the prior art) to introduce conventional deposit-control fuel additives into the fuel composition. It can be seen that, the deposit-control fuel additives pass directly from the deposit-control fuel additive source (16') via a line (24') to a fuel blending point (32').
  • the octane-boosting additive blending system of the present invention may be used to supplement a conventional deposit-control additive blending system.
  • the additives were added to the fuel at a relatively low treat rate of 0.67 % weight additive / weight base fuel, equivalent to a treat rate of 5 g additive / litre of fuel.
  • the fuel was an E10 gasoline base fuel.
  • the RON and MON of the base fuel, as well as the blends of base fuel and octane-boosting additive, were determined according to ASTM D2699 and ASTM D2700, respectively.
  • the octane-boosting additives may be used to increase the RON of an oxygenate fuel for a spark-ignition internal combustion engine.
  • Example 1 Further additives from Example 1 (OX4, OX10, OX11, OX14, OX15, OX16 and OX18) were tested in the E10 gasoline base fuel. Each of the additives increased the RON of the fuel.
  • Example 3 Variation of octane number with octane-boosting additive treat rate
  • the fuel was an E10 gasoline base fuel.
  • the RON and MON of the base fuel, as well as the blends of base fuel and octane-boosting additive, were determined according to ASTM D2699 and ASTM D2700, respectively.
  • FIG. 2 A graph of the effect of the octane-boosting additive on the RON and MON of the fuel is shown in Figure 2 . It can be seen that the octane-boosting additive had a significant effect on the octane numbers of the fuel, even at very low treat rates.
  • the RON and MON of the base fuels, as well as the blends of base fuel and octane-boosting additive, were determined according to ASTM D2699 and ASTM D2700, respectively.
  • FIG. 3a A graph of the change in octane number of the E10 fuel against treat rate of N-methyl aniline and an octane-boosting additive (OX6) is shown in Figure 3a .
  • the treat rates are typical of those used in a fuel. It can be seen from the graph that the performance of the octane-boosting additives described herein is significantly better than that of N-methyl aniline across the treat rates.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
EP16155208.8A 2016-02-11 2016-02-11 Additising a fuel Withdrawn EP3205700A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
EP16155208.8A EP3205700A1 (en) 2016-02-11 2016-02-11 Additising a fuel
EP17703196.0A EP3414304A1 (en) 2016-02-11 2017-02-09 Additising a fuel
PCT/EP2017/052926 WO2017137516A1 (en) 2016-02-11 2017-02-09 Additising a fuel
MX2018009649A MX2018009649A (es) 2016-02-11 2017-02-09 Addicion de un combustible.
CN201780011021.5A CN109072106A (zh) 2016-02-11 2017-02-09 对燃料进行添加处理
EA201891777A EA201891777A1 (ru) 2016-02-11 2017-02-09 Добавление присадок в топливо
CA3013661A CA3013661A1 (en) 2016-02-11 2017-02-09 Additising a fuel
AU2017218511A AU2017218511A1 (en) 2016-02-11 2017-02-09 Additising a fuel
BR112018016436-4A BR112018016436B1 (pt) 2016-02-11 2017-02-09 Método para preparar uma composição de combustível, oxigenato aditivado e método para produzir oxigenato aditivado
SG11201806710VA SG11201806710VA (en) 2016-02-11 2017-02-09 Additising a fuel
JP2018542192A JP2019509372A (ja) 2016-02-11 2017-02-09 燃料への添加剤の添加
US16/077,450 US10927320B2 (en) 2016-02-11 2017-02-09 Additising a fuel

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EP16155208.8A EP3205700A1 (en) 2016-02-11 2016-02-11 Additising a fuel

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BR (1) BR112018016436B1 (es)
CA (1) CA3013661A1 (es)
EA (1) EA201891777A1 (es)
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2021507929A (ja) * 2017-12-27 2021-02-25 ビーピー オイル インターナショナル リミテッドＢｐ Ｏｉｌ Ｉｎｔｅｒｎａｔｉｏｎａｌ Ｌｉｍｉｔｅｄ 燃料添加物の調製方法

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201713023D0 (en) 2017-08-14 2017-09-27 Bp Oil Int Ltd Methods for blending fuels
GB201713009D0 (en) 2017-08-14 2017-09-27 Bp Oil Int Ltd Methods for reducing oxidation
GB201713019D0 (en) 2017-08-14 2017-09-27 Bp Oil Int Ltd Methods for controlling deposits
EP3828253A1 (en) * 2019-11-29 2021-06-02 BP Oil International Limited Low greenhouse gas fuel compositions
AU2022316323A1 (en) 2021-07-21 2023-12-14 Topsoe A/S Process and plant for improving gasoline octane rating

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2308849A (en) * 1996-01-08 1997-07-09 Ass Octel Anti-knock additive
WO2005087901A2 (en) * 2004-03-09 2005-09-22 Innospec Limited Fuel additive composition having antiknock properties
US20100269404A1 (en) * 2005-01-18 2010-10-28 Bestline International Research Inc. Universal Synthetic Gasoline Fuel Conditioner Additive, Method and Product-by-Process

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1833429A (en) * 1929-08-28 1931-11-24 Gen Motors Res Corp Method and means for removing carbon deposits
US20070204505A1 (en) * 2006-03-02 2007-09-06 Novus International Inc. Gasoline fuel compositions having increased oxidative stability

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2308849A (en) * 1996-01-08 1997-07-09 Ass Octel Anti-knock additive
WO2005087901A2 (en) * 2004-03-09 2005-09-22 Innospec Limited Fuel additive composition having antiknock properties
US20100269404A1 (en) * 2005-01-18 2010-10-28 Bestline International Research Inc. Universal Synthetic Gasoline Fuel Conditioner Additive, Method and Product-by-Process

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2021507929A (ja) * 2017-12-27 2021-02-25 ビーピー オイル インターナショナル リミテッドＢｐ Ｏｉｌ Ｉｎｔｅｒｎａｔｉｏｎａｌ Ｌｉｍｉｔｅｄ 燃料添加物の調製方法

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MX2018009649A (es) 2019-01-31
JP2019509372A (ja) 2019-04-04
BR112018016436A2 (pt) 2018-12-26
WO2017137516A1 (en) 2017-08-17
EP3414304A1 (en) 2018-12-19
US10927320B2 (en) 2021-02-23
BR112018016436B1 (pt) 2022-02-22
US20190040331A1 (en) 2019-02-07
CA3013661A1 (en) 2017-08-17
SG11201806710VA (en) 2018-09-27
EA201891777A1 (ru) 2019-03-29
AU2017218511A1 (en) 2018-08-16

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